Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 400916
  • Symbol: CHCHD10
  • Description: coiled-coil-helix-coiled-coil-helix domain containing 10

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Disease_Term Source Rank Other Values
?Myopathy, isolated mitochondrial, autosomal dominant, 616209 (3) OMIM high
  • Genome region : 22q11.23
  • OMIM_ID : 615903 OMIM gene ID
  • OMIM_ID : 616209 OMIM phenotype ID
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, 615911 (3) OMIM high
  • Genome region : 22q11.23
  • OMIM_ID : 615903 OMIM gene ID
  • OMIM_ID : 615911 OMIM phenotype ID
Spinal muscular atrophy, Jokela type, 615048 (3) OMIM high
  • Genome region : 22q11.23
  • OMIM_ID : 615048 OMIM phenotype ID
  • OMIM_ID : 615903 OMIM gene ID